Canonical Allele Identifier: CA2410906036

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50524009_50524011delinsCAG , CM000684.2:g.50524009_50524011delinsCAG GRCh38
NC_000022.10:g.50962438_50962440delinsCAG , CM000684.1:g.50962438_50962440delinsCAG GRCh37
NC_000022.9:g.49309304_49309306delinsCAG NCBI36
NG_011860.1:g.11075_11077delinsCTG , LRG_727:g.11075_11077delinsCTG
NG_016235.1:g.7429_7431delinsCTG
NG_021419.1:g.20794_20796delinsCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000395693.8:c.401_403delinsCTG (SCO2) MANE Select ENSP00000379046.4:p.Pro134=
ENST00000420993.7:c.*634_*636delinsCAG (NCAPH2) MANE Select ENSP00000410088.2:n.*634_*636delinsCAG
ENST00000543927.6:c.401_403delinsCTG (SCO2) ENSP00000444433.1:p.Pro134=
ENST00000638598.2:c.401_403delinsCTG (SCO2) ENSP00000491753.2:p.Pro134=
ENST00000252785.3:c.401_403delinsCTG ENSP00000252785.3:p.Pro134=
ENST00000395693.7:c.401_403delinsCTG ENSP00000379046.3:p.Pro134=
ENST00000423348.1:c.401_403delinsCTG ENSP00000403570.1:p.Pro134=
ENST00000439934.5:c.401_403delinsCTG ENSP00000415642.1:p.Pro134=
ENST00000535425.5:c.401_403delinsCTG ENSP00000444242.1:p.Pro134=
ENST00000543927.5:c.401_403delinsCTG ENSP00000444433.1:p.Pro134=
NM_001169109.1:c.401_403delinsCTG (SCO2) NP_001162580.1:p.Pro134=
NM_001169110.1:c.401_403delinsCTG (SCO2) NP_001162581.1:p.Pro134=
NM_001169111.1:c.401_403delinsCTG (SCO2) NP_001162582.1:p.Pro134=
NM_001185011.1:c.*634_*636delinsCAG (NCAPH2) NP_001171940.1:n.*634_*636delinsCAG
NM_005138.2:c.401_403delinsCTG (SCO2) NP_005129.2:p.Pro134=
NM_152299.3:c.*634_*636delinsCAG (NCAPH2) NP_689512.2:n.*634_*636delinsCAG
XR_001755232.1:n.2662_2664delinsCAG (NCAPH2)
NM_152299.4:c.*634_*636delinsCAG (NCAPH2) MANE Select NP_689512.2:n.*634_*636delinsCAG
NM_001185011.2:c.*634_*636delinsCAG (NCAPH2) NP_001171940.1:n.*634_*636delinsCAG
NM_005138.3:c.401_403delinsCTG (SCO2) MANE Select NP_005129.2:p.Pro134=
NM_001169109.2:c.401_403delinsCTG (SCO2) NP_001162580.1:p.Pro134=
NM_001169111.2:c.401_403delinsCTG (SCO2) NP_001162582.1:p.Pro134=